Mesenteric Lymphangioma – a Rare Tumor of the Abdomen

Mesenteric lymphangioma (ML) is a cystic tumor developed at the base of the mesentery, which occurs frequently in children, rarely in adults, with nonspecific symptoms, often diagnosed late. The diagnosis is made by computer tomography and the curative treatment is the surgical one with good results...

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Main Authors: Florin BOBIRCA, Ionut MELESTEU, Dan DUMITRESCU1, Carmen IORGUS, Romina Marina SIMA, Traian PATRASCU, Anca BOBIRCA
Format: Article
Language:English
Published: Bucharest College of Physicians 2022-06-01
Series:Modern Medicine
Subjects:
Online Access:https://medicinamoderna.ro/wp-content/uploads/2022/06/Mesenteric-Lymphangioma-%E2%80%93-a-Rare-Tumor-of-the-Abdomen-art-10.pdf
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author Florin BOBIRCA
Ionut MELESTEU
Dan DUMITRESCU1
Carmen IORGUS
Romina Marina SIMA
Traian PATRASCU
Anca BOBIRCA
author_facet Florin BOBIRCA
Ionut MELESTEU
Dan DUMITRESCU1
Carmen IORGUS
Romina Marina SIMA
Traian PATRASCU
Anca BOBIRCA
author_sort Florin BOBIRCA
collection DOAJ
description Mesenteric lymphangioma (ML) is a cystic tumor developed at the base of the mesentery, which occurs frequently in children, rarely in adults, with nonspecific symptoms, often diagnosed late. The diagnosis is made by computer tomography and the curative treatment is the surgical one with good results and with optimal postoperative outcome. A 44-year-old patient for whom mesh surgery for incisional hernia post appendectomy has been performed was admitted to our clinic for nonspecific gastrointestinal symptoms for which he has also been investigated multiple times in other services. On the right flank and iliac fossa, a tumor of firmelastic consistency is detected, relatively well delimited. Computed tomography (CT) describes the lesion as a mesenteric tumor. Intraoperatively, a cystic tumor is detected, which is punctured, the biochemical result highlighting the lymphatic character. The surgical treatment was represented by segmental intestinal resection with entero-enteroanastomosis. No postoperative events were reported.
format Article
id doaj-art-e373142750f64ba0a156b9c49b9501a1
institution Kabale University
issn 1223-0472
2360-2473
language English
publishDate 2022-06-01
publisher Bucharest College of Physicians
record_format Article
series Modern Medicine
spelling doaj-art-e373142750f64ba0a156b9c49b9501a12025-08-20T03:48:36ZengBucharest College of PhysiciansModern Medicine1223-04722360-24732022-06-01292165167https://doi.org/10.31689/rmm.2021.29.2.165Mesenteric Lymphangioma – a Rare Tumor of the AbdomenFlorin BOBIRCA0https://orcid.org/0000-0002-8944-3857Ionut MELESTEU1Dan DUMITRESCU12https://orcid.org/0000-0001-8413-0977Carmen IORGUS3Romina Marina SIMA4https://orcid.org/0000-0002-9541-3347Traian PATRASCU5Anca BOBIRCA6https://orcid.org/0000-0002-6662-7354”Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaDepartment of Gastroenterology, Colentina Clinical Hospital, Bucharest, Romania”Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaDepartment of Internal Medicine and Rheumatology, „Dr Ion Cantacuzino” Clinical Hospital, Bucharest, RomaniaDepartment of Obstetrics and Gynecology, ”Sf. Ioan” Clinical Hospital, Bucharest, Romania”Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania”Carol Davila” University of Medicine and Pharmacy, Bucharest, RomaniaMesenteric lymphangioma (ML) is a cystic tumor developed at the base of the mesentery, which occurs frequently in children, rarely in adults, with nonspecific symptoms, often diagnosed late. The diagnosis is made by computer tomography and the curative treatment is the surgical one with good results and with optimal postoperative outcome. A 44-year-old patient for whom mesh surgery for incisional hernia post appendectomy has been performed was admitted to our clinic for nonspecific gastrointestinal symptoms for which he has also been investigated multiple times in other services. On the right flank and iliac fossa, a tumor of firmelastic consistency is detected, relatively well delimited. Computed tomography (CT) describes the lesion as a mesenteric tumor. Intraoperatively, a cystic tumor is detected, which is punctured, the biochemical result highlighting the lymphatic character. The surgical treatment was represented by segmental intestinal resection with entero-enteroanastomosis. No postoperative events were reported.https://medicinamoderna.ro/wp-content/uploads/2022/06/Mesenteric-Lymphangioma-%E2%80%93-a-Rare-Tumor-of-the-Abdomen-art-10.pdfmesenteric lymphangiomacystic tumorsurgical treatment
spellingShingle Florin BOBIRCA
Ionut MELESTEU
Dan DUMITRESCU1
Carmen IORGUS
Romina Marina SIMA
Traian PATRASCU
Anca BOBIRCA
Mesenteric Lymphangioma – a Rare Tumor of the Abdomen
Modern Medicine
mesenteric lymphangioma
cystic tumor
surgical treatment
title Mesenteric Lymphangioma – a Rare Tumor of the Abdomen
title_full Mesenteric Lymphangioma – a Rare Tumor of the Abdomen
title_fullStr Mesenteric Lymphangioma – a Rare Tumor of the Abdomen
title_full_unstemmed Mesenteric Lymphangioma – a Rare Tumor of the Abdomen
title_short Mesenteric Lymphangioma – a Rare Tumor of the Abdomen
title_sort mesenteric lymphangioma a rare tumor of the abdomen
topic mesenteric lymphangioma
cystic tumor
surgical treatment
url https://medicinamoderna.ro/wp-content/uploads/2022/06/Mesenteric-Lymphangioma-%E2%80%93-a-Rare-Tumor-of-the-Abdomen-art-10.pdf
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AT dandumitrescu1 mesentericlymphangiomaararetumoroftheabdomen
AT carmeniorgus mesentericlymphangiomaararetumoroftheabdomen
AT rominamarinasima mesentericlymphangiomaararetumoroftheabdomen
AT traianpatrascu mesentericlymphangiomaararetumoroftheabdomen
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